- Using GC-MS LC-MS and/or ICP-MS to support commercial and clinical testing of extractables and leachables for pharmaceutical manufacturing following all pertinent protocols and standard operating procedures (SOPs).
- Generate compile and process complex data.
- Reviews test results to ensure compliance with standards; reports any quality anomalies.
- Use processed and historical data to support conclusions and author technical summary documents of test results.
- Calibrates or verifies calibration of instruments/devices prior to use.
- Troubleshooting instrumentation and lab techniques when appropriate.
- Comply with all pertinent regulatory agency requirements.
- Follows all current cGxP (e.g. good manufacturing processes good documentation practices etc.)
- Participates in required training activities as both trainee and trainer.
- Maintains laboratory supplies safety and compliance.
- Interacts with outside vendors and/or functional peer groups in a professional manner.
- May assist in validation of methods
- Excellent communication (oral and written) and attention to detail.
- Ability to work independently and as part of a team self-motivated adaptability and a positive attitude
- Ability to learn new techniques perform multiple tasks simultaneously keep accurate records follow instructions and comply with company policies
Leadership Responsibilities
- Supports and monitors performance of team of employees
- Monitors the day to day operations of QC analyst staff
- May participate in new hire interviews
- Supports the on-boarding process of new employees
- Facilitate staff access to systems controlled areas etc. using approved procedures
- Participates in training of other employees.
- Performs peer review of data.
- May support peer group lead operations
- Assists in coordinating equipment maintenance and calibration.
- Disseminate administrative communications
- Demonstrate and promote the company vision
- Meet all quality and productivity metrics and demonstrate strong teamwork and collaboration
- Participate in productivity tracking and prepares monthly metrics and quality reports.
- Coordinate scheduling and allocation of responsibilities and new hire on-boarding process
- Coordinates training program
Qualifications :
The Ideal Candidate would possess:
- Strong leadership and teambuilding skills
- Familiarity with Lean or 5s or Operational Excellence
- Excellent communication (oral and written) and attention to detail
- Ability to work independently and as part of a team self-motivation adaptability and a positive attitude
- Ability to learn new techniques perform multiple tasks simultaneously keep accurate records follow instructions and comply with company policies
Minimum Qualifications
- Bachelors degree in chemistry (or other science related degree concentration) with 2 years of industry experience or Masters degree with any industry experience
- Experience in GC-MS LC-MS and/or ICP-MS
- Experience operating inside of a GMP lab space
- 1-2 years of previous dynamic team leadership experience
- Strong computer scientific and organizational skills
- Experience writing and reviewing detailed technical documents
- Experience with an electronic laboratory information management system
- Authorization to work in the United States indefinitely without restriction or sponsorship
Additional Information :
What to Expect in the Hiring Process:
- 10-15 Minute Phone Interview with Region Recruiter
- 45-60 Minute Virtual Interview with Manager and/or Group Leader
- 30 Minute Virtual Interview with Site Director
Additional Details:
The position is full-time first shift Monday-Friday from 8am-4:30pm. Candidates must be flexible to adapt to schedule changes that may require shift changes and/or weekend work and overtime may be required as needed. Candidates living within a commutable distance of Rensselaer New York are encouraged to apply.
Excellent full-time benefits include:
- comprehensive medical coverage dental and vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holiday
- Yearly goal-based bonus & eligibility for merit-based increases
- Pay is between 29.00-32.00
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.
Remote Work :
No
Employment Type :
Full-time
Using GC-MS LC-MS and/or ICP-MS to support commercial and clinical testing of extractables and leachables for pharmaceutical manufacturing following all pertinent protocols and standard operating procedures (SOPs).Generate compile and process complex data.Reviews test results to ensure compliance wi...
- Using GC-MS LC-MS and/or ICP-MS to support commercial and clinical testing of extractables and leachables for pharmaceutical manufacturing following all pertinent protocols and standard operating procedures (SOPs).
- Generate compile and process complex data.
- Reviews test results to ensure compliance with standards; reports any quality anomalies.
- Use processed and historical data to support conclusions and author technical summary documents of test results.
- Calibrates or verifies calibration of instruments/devices prior to use.
- Troubleshooting instrumentation and lab techniques when appropriate.
- Comply with all pertinent regulatory agency requirements.
- Follows all current cGxP (e.g. good manufacturing processes good documentation practices etc.)
- Participates in required training activities as both trainee and trainer.
- Maintains laboratory supplies safety and compliance.
- Interacts with outside vendors and/or functional peer groups in a professional manner.
- May assist in validation of methods
- Excellent communication (oral and written) and attention to detail.
- Ability to work independently and as part of a team self-motivated adaptability and a positive attitude
- Ability to learn new techniques perform multiple tasks simultaneously keep accurate records follow instructions and comply with company policies
Leadership Responsibilities
- Supports and monitors performance of team of employees
- Monitors the day to day operations of QC analyst staff
- May participate in new hire interviews
- Supports the on-boarding process of new employees
- Facilitate staff access to systems controlled areas etc. using approved procedures
- Participates in training of other employees.
- Performs peer review of data.
- May support peer group lead operations
- Assists in coordinating equipment maintenance and calibration.
- Disseminate administrative communications
- Demonstrate and promote the company vision
- Meet all quality and productivity metrics and demonstrate strong teamwork and collaboration
- Participate in productivity tracking and prepares monthly metrics and quality reports.
- Coordinate scheduling and allocation of responsibilities and new hire on-boarding process
- Coordinates training program
Qualifications :
The Ideal Candidate would possess:
- Strong leadership and teambuilding skills
- Familiarity with Lean or 5s or Operational Excellence
- Excellent communication (oral and written) and attention to detail
- Ability to work independently and as part of a team self-motivation adaptability and a positive attitude
- Ability to learn new techniques perform multiple tasks simultaneously keep accurate records follow instructions and comply with company policies
Minimum Qualifications
- Bachelors degree in chemistry (or other science related degree concentration) with 2 years of industry experience or Masters degree with any industry experience
- Experience in GC-MS LC-MS and/or ICP-MS
- Experience operating inside of a GMP lab space
- 1-2 years of previous dynamic team leadership experience
- Strong computer scientific and organizational skills
- Experience writing and reviewing detailed technical documents
- Experience with an electronic laboratory information management system
- Authorization to work in the United States indefinitely without restriction or sponsorship
Additional Information :
What to Expect in the Hiring Process:
- 10-15 Minute Phone Interview with Region Recruiter
- 45-60 Minute Virtual Interview with Manager and/or Group Leader
- 30 Minute Virtual Interview with Site Director
Additional Details:
The position is full-time first shift Monday-Friday from 8am-4:30pm. Candidates must be flexible to adapt to schedule changes that may require shift changes and/or weekend work and overtime may be required as needed. Candidates living within a commutable distance of Rensselaer New York are encouraged to apply.
Excellent full-time benefits include:
- comprehensive medical coverage dental and vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holiday
- Yearly goal-based bonus & eligibility for merit-based increases
- Pay is between 29.00-32.00
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.
Remote Work :
No
Employment Type :
Full-time
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